Canonical Allele Identifier: CA389413247

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269468T>A (hg19) ; chr14:g.33800262T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800262T>A , CM000676.2:g.33800262T>A	GRCh38
NC_000014.8:g.34269468T>A , CM000676.1:g.34269468T>A	GRCh37
NC_000014.7:g.33339219T>A	NCBI36
NG_013036.1:g.866010T>A
NG_013036.2:g.866010T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1955T>A MANE Select	ENSP00000348460.4:p.Ile652Asn
ENST00000551634.6:c.1964T>A	ENSP00000448373.2:p.Ile655Asn
ENST00000680362.1:c.1855T>A
ENST00000681323.1:c.793+2681T>A
ENST00000346562.6:c.1859T>A	ENSP00000319610.5:p.Ile620Asn
ENST00000356141.8:c.1955T>A	ENSP00000348460.4:p.Ile652Asn
ENST00000357798.9:c.1916T>A	ENSP00000350446.5:p.Ile639Asn
ENST00000548645.5:c.1865T>A	ENSP00000448916.1:p.Ile622Asn
ENST00000551492.5:c.1970T>A	ENSP00000450392.1:p.Ile657Asn
ENST00000551634.5:c.1877T>A	ENSP00000448373.1:p.Ile626Asn
NM_001164749.1:c.1955T>A	NP_001158221.1:p.Ile652Asn
NM_001165893.1:c.1865T>A	NP_001159365.1:p.Ile622Asn
NM_022123.2:c.1859T>A	NP_071406.1:p.Ile620Asn
NM_173159.2:c.1916T>A	NP_775182.1:p.Ile639Asn
XM_005267991.2:c.1976T>A	XP_005268048.1:p.Ile659Asn
XM_005267992.2:c.1970T>A	XP_005268049.1:p.Ile657Asn
XM_005267993.2:c.1916T>A	XP_005268050.1:p.Ile639Asn
XM_011537067.1:c.2006T>A	XP_011535369.1:p.Ile669Asn
XM_011537068.1:c.1997T>A	XP_011535370.1:p.Ile666Asn
XM_011537069.1:c.1967T>A	XP_011535371.1:p.Ile656Asn
XM_011537070.1:c.1910T>A	XP_011535372.1:p.Ile637Asn
XM_011537071.1:c.1877T>A	XP_011535373.1:p.Ile626Asn
XM_011537072.1:c.1856T>A	XP_011535374.1:p.Ile619Asn
XM_011537073.1:c.1649T>A	XP_011535375.1:p.Ile550Asn
XM_011537074.1:c.1649T>A	XP_011535376.1:p.Ile550Asn
XM_005267991.3:c.2063T>A	XP_005268048.2:p.Ile688Asn
XM_005267992.3:c.2057T>A	XP_005268049.2:p.Ile686Asn
XM_011537067.2:c.2006T>A	XP_011535369.1:p.Ile669Asn
XM_011537069.2:c.2054T>A	XP_011535371.2:p.Ile685Asn
XM_011537070.2:c.1910T>A	XP_011535372.1:p.Ile637Asn
XM_011537071.2:c.1964T>A	XP_011535373.2:p.Ile655Asn
XM_011537072.2:c.1856T>A	XP_011535374.1:p.Ile619Asn
XM_017021582.1:c.2114T>A	XP_016877071.1:p.Ile705Asn
XM_017021583.1:c.2105T>A	XP_016877072.1:p.Ile702Asn
XM_017021584.1:c.2024T>A	XP_016877073.1:p.Ile675Asn
XM_017021585.1:c.1973T>A	XP_016877074.1:p.Ile658Asn
XM_017021586.1:c.1649T>A	XP_016877075.1:p.Ile550Asn
XM_017021587.1:c.1649T>A	XP_016877076.1:p.Ile550Asn
XM_017021588.1:c.1649T>A	XP_016877077.1:p.Ile550Asn
NM_001164749.2:c.1955T>A MANE Select	NP_001158221.1:p.Ile652Asn
NM_001165893.2:c.1865T>A	NP_001159365.1:p.Ile622Asn
NM_022123.3:c.1859T>A	NP_071406.1:p.Ile620Asn
NM_173159.3:c.1916T>A	NP_775182.1:p.Ile639Asn
NM_001394988.1:c.1910T>A	NP_001381917.1:p.Ile637Asn
NM_001394989.1:c.1856T>A	NP_001381918.1:p.Ile619Asn